Canonical Allele Identifier: CA2519439745

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340702_45340704del , CM000663.2:g.45340702_45340704del GRCh38
NC_000001.10:g.45806374_45806376del , CM000663.1:g.45806374_45806376del GRCh37
NC_000001.9:g.45578961_45578963del NCBI36
NG_008189.1:g.4771_4773del , LRG_220:g.4771_4773del

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.53-371_53-369del (TOE1) MANE Select ENSP00000361162.5:n.53-371_53-369del
ENST00000671898.1:c.541-6189_541-6187del ENSP00000499896.1:n.541-6189_541-6187del
ENST00000672011.1:c.-446_-444del (MUTYH) ENSP00000500418.1:n.-446_-444del
ENST00000372090.5:c.53-371_53-369del (TOE1) ENSP00000361162.5:n.53-371_53-369del
ENST00000471337.5:n.131-371_131-369del (TOE1)
ENST00000477731.5:n.272-371_272-369del (TOE1)
ENST00000495703.5:n.322+160_322+162del (TOE1)
NM_025077.3:c.53-371_53-369del (TOE1) NP_079353.3:n.53-371_53-369del
XM_005270412.2:c.71-371_71-369del (TOE1) XP_005270469.1:n.71-371_71-369del
XM_005270413.3:c.-87+160_-87+162del (TOE1) XP_005270470.1:n.-87+160_-87+162del
XM_011540569.1:c.-232-371_-232-369del (TOE1) XP_011538871.1:n.-232-371_-232-369del
XR_246230.2:n.330-371_330-369del (TOE1)
XR_426587.2:n.150-371_150-369del (TOE1)
XR_946532.1:n.150-371_150-369del (TOE1)
XM_005270412.4:c.71-371_71-369del (TOE1) XP_005270469.1:n.71-371_71-369del
XM_005270413.5:c.-87+160_-87+162del (TOE1) XP_005270470.1:n.-87+160_-87+162del
XM_011540569.3:c.-232-371_-232-369del (TOE1) XP_011538871.1:n.-232-371_-232-369del
XM_024452837.1:c.-87+160_-87+162del (TOE1) XP_024308605.1:n.-87+160_-87+162del
XR_001736951.2:n.240-371_240-369del (TOE1)
XR_002959287.1:n.555-371_555-369del (TOE1)
XR_246230.4:n.240-371_240-369del (TOE1)
XR_426587.4:n.150-371_150-369del (TOE1)
XR_946532.3:n.150-371_150-369del (TOE1)
NM_025077.4:c.53-371_53-369del (TOE1) MANE Select NP_079353.3:n.53-371_53-369del